GenotypeAsAModelOfDiseaseAssociation
None
classDiagram
ModelToDiseaseAssociationMixin <|-- GenotypeAsAModelOfDiseaseAssociation
EntityToDiseaseAssociationMixin <|-- GenotypeAsAModelOfDiseaseAssociation
GenotypeToDiseaseAssociation <|-- GenotypeAsAModelOfDiseaseAssociation
GenotypeAsAModelOfDiseaseAssociation : aggregator_knowledge_source
GenotypeAsAModelOfDiseaseAssociation : category
GenotypeAsAModelOfDiseaseAssociation : description
GenotypeAsAModelOfDiseaseAssociation : frequency_qualifier
GenotypeAsAModelOfDiseaseAssociation : has_attribute
GenotypeAsAModelOfDiseaseAssociation : has_evidence
GenotypeAsAModelOfDiseaseAssociation : id
GenotypeAsAModelOfDiseaseAssociation : iri
GenotypeAsAModelOfDiseaseAssociation : knowledge_source
GenotypeAsAModelOfDiseaseAssociation : name
GenotypeAsAModelOfDiseaseAssociation : negated
GenotypeAsAModelOfDiseaseAssociation : object
GenotypeAsAModelOfDiseaseAssociation : onset_qualifier
GenotypeAsAModelOfDiseaseAssociation : original_knowledge_source
GenotypeAsAModelOfDiseaseAssociation : predicate
GenotypeAsAModelOfDiseaseAssociation : primary_knowledge_source
GenotypeAsAModelOfDiseaseAssociation : publications
GenotypeAsAModelOfDiseaseAssociation : qualifiers
GenotypeAsAModelOfDiseaseAssociation : severity_qualifier
GenotypeAsAModelOfDiseaseAssociation : source
GenotypeAsAModelOfDiseaseAssociation : subject
GenotypeAsAModelOfDiseaseAssociation : timepoint
GenotypeAsAModelOfDiseaseAssociation : type
Parent Classes
- Entity
- Association
- GenotypeToDiseaseAssociation [ genotype to entity association mixin entity to disease association mixin]
- GenotypeAsAModelOfDiseaseAssociation [ model to disease association mixin entity to disease association mixin]
- GenotypeToDiseaseAssociation [ genotype to entity association mixin entity to disease association mixin]
- Association
Slots
Name | Description |
---|---|
aggregator_knowledge_source | An intermediate aggregator resource from which knowledge expressed in an Association was retrieved downstream of the original source, on its path to its current serialized form. |
category | Name of the high level ontology class in which this entity is categorized. Corresponds to the label for the biolink entity type class. In a neo4j database this MAY correspond to the neo4j label tag. In an RDF database it should be a biolink model class URI. This field is multi-valued. It should include values for ancestors of the biolink class; for example, a protein such as Shh would have category values biolink:Protein , biolink:GeneProduct , biolink:MolecularEntity , etc. In an RDF database, nodes will typically have an rdf:type triples. This can be to the most specific biolink class, or potentially to a class more specific than something in biolink. For example, a sequence feature f may have a rdf:type assertion to a SO class such as TF_binding_site, which is more specific than anything in biolink. Here we would have categories {biolink:GenomicEntity, biolink:MolecularEntity, biolink:NamedThing} |
description | a human-readable description of an entity |
frequency_qualifier | a qualifier used in a phenotypic association to state how frequent the phenotype is observed in the subject |
has_attribute | connects any entity to an attribute |
has_evidence | connects an association to an instance of supporting evidence |
id | A unique identifier for an entity. Must be either a CURIE shorthand for a URI or a complete URI |
iri | An IRI for an entity. This is determined by the id using expansion rules. |
knowledge_source | An Information Resource from which the knowledge expressed in an Association was retrieved, directly or indirectly. This can be any resource through which the knowledge passed on its way to its currently serialized form. In practice, implementers should use one of the more specific subtypes of this generic property. |
name | A human-readable name for an attribute or entity. |
negated | if set to true, then the association is negated i.e. is not true |
object | connects an association to the object of the association. For example, in a gene-to-phenotype association, the gene is subject and phenotype is object. |
onset_qualifier | a qualifier used in a phenotypic association to state when the phenotype appears is in the subject |
original_knowledge_source | None |
predicate | A high-level grouping for the relationship type. AKA minimal predicate. This is analogous to category for nodes. |
primary_knowledge_source | The most upstream source of the knowledge expressed in an Association that an implementer can identify (may or may not be the 'original' source). |
publications | connects an association to publications supporting the association |
qualifiers | connects an association to qualifiers that modify or qualify the meaning of that association |
severity_qualifier | a qualifier used in a phenotypic association to state how severe the phenotype is in the subject |
source | None |
subject | A genotype that has a role in modeling the disease. |
timepoint | a point in time |
type | None |
Mappings
Mapping Type | Mapped Value |
---|---|
self | ['biolink:GenotypeAsAModelOfDiseaseAssociation'] |
native | ['biolink:GenotypeAsAModelOfDiseaseAssociation'] |